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Havel's

FDA UDI

Class II (US FDA UDI)

by Havel's Incorporated

Identity

Trade Name
HAVEL'S FDA UDI
Generic Name
Silk suture FDA UDI
Device Name
SUTURE 4-0 SILK BLK 18"/DS-12 FDA UDI
Model / Reference
SUT. 4-0 SILK BLK 18"/DS-12 FDA UDI
Description
SUTURE 4-0 SILK BLK 18"/DS-12 FDA UDI

Identifiers

Catalog Number
B77D FDA UDI
Primary DI / UDI-DI
B070B77D0 FDA UDI
FDA Product Code
GAP FDA UDI
GMDN Term
Silk suture FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Silk suture

Havel's by Havel's Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silk suture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 481dc0c8-bf85-4a31-910c-fc83bce699ac 35 fields · synced May 30, 2026